My Great Strides Story
Growing up with undiagnosed cystic fibrosis, I always knew I was different but was unable to find answers or supports. I have been sick throughout most of my life and often feel depleted. I have often felt I needed to tough it out and push through even when my body told me it couldn’t.
After being diagnosed with cystic fibrosis at the age of 36, I have realized that the symptoms I’ve struggled with is part of living with a chronic illness. My recent diagnosis has evoked a period of pain but also of validation. Looking back it all makes sense now and I feel a justification around me. My journey to recovery has been life-changing and challenging, but has given me a lot of strength and much needed resources.
I am having to learn how to give myself time to rest and to listen to my body. My diagnosis is new and raw and difficult for me to share. I am doing it despite this because the CF foundation has given me the help and guidance I need as I learn about and navigate through my CF.
The CF Foundation has supported me with information, resources, financial support, and a community. I am proud to walk to support those with CF and look forward to your support either walking along side me or with your financial support! Thank you for helping me make a difference!!
Your support makes a difference.
There is no cure for CF, but there is help and there is hope. By donating to this cause you are helping people like me get the resources they need to feel their best and live their lives to the fullest they can. Thank you for your help and support!
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.